Autosomal dominant cerebellar ataxia type I in Martinique (French West Indies) : clinical and neuropathological analysis of 53 patients from three unrelated SCA2 families

Autosomal dominant cerebellar ataxia type I was diagnosed in three unrelated families from Martinique (French West Indies), and linkage to the locus for spinocerebellar ataxia 2 (SCA2) was established. Neuropathological findings in two patients were those of olivopontocerebellar atrophy without olig...

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Veröffentlicht in:	Brain (London, England : 1878) England : 1878), 1995-12, Vol.118 (6), p.1573-1581
Hauptverfasser:	DÜRR, A, SMADJA, D, AGID, Y, BRICE, A, VERNANT, J.-C, CANCEL, G, LEZIN, A, STEVANIN, G, MIKOL, J, BELLANCE, R, BUISSON, G.-G, CHNEIWEISS, H, DELLANAVE, J
Format:	Artikel
Sprache:	eng
Schlagworte:	Adolescent Adult Age of Onset Aged Biological and medical sciences Brain - pathology Cerebellar Ataxia - genetics Cerebellar Ataxia - pathology Cerebellar Ataxia - physiopathology Child Disorders of higher nervous function. Focal brain diseases. Central vestibular syndrome and deafness. Brain stem syndromes Female Genes, Dominant Humans Male Martinique Medical sciences Middle Aged Nervous system (semeiology, syndromes) Neurology Pedigree Phenotype
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